Post-operative Use of New Adhesive After Total Laryngectomy

Starting soon · Not applicable

Conditions studied: Laryngectomy

In brief

The goal of this clinical trial is to evaluate the feasibility, safety, and performance of the new adhesive when used in the immediate post-operative period after total laryngectomy. The main question it aims to answer is: \- Is the adhesive feasible and safe to use during the early post-operative phase? This is a single-arm feasibility study with historical controls, so there is no concurrent comparison group. Researchers will compare outcomes to historical data from standard adhesive use to assess improvements in tolerance and skin condition. Participants will: * Use the adhesive as part of their standard post-laryngectomy care. * Complete patient-reported outcome questionnaires (e.g., comfort, skin assessment, satisfaction). * Allow investigators to record observations in diaries and patient charts. * Participate in routine clinical assessments during hospitalization and at end of study (approximately 30 days post-surgery).

Key facts

Study ID

NCT07366281

Run by

Atos Medical AB

People needed

25

Starts

2026-08-17

Expected to finish

2027-08-01

Last updated by the study team

2026-07-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient undergoing total laryngectomy surgery
• 18 years or older

You may not qualify if…

• Unable to give informed consent prior to TL surgery

Where it is running

• Antoni van Leeuwenhoek, Netherlands Cancer Institute — Amsterdam, Netherlands

Full record on ClinicalTrials.gov

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